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. 2016 Jul 15;5:212297. doi: 10.7573/dic.212297

Table 2.

Clinical inputs.

N+I [source] D+T [source]
Efficacy inputs
ORR in % [source] 67.0% [15] 69% [6]
Median PFS in months [source] 11.7 [10] 11.0 [6]
Grade 3 and 4 adverse events N+I pooled RCT AEs in % [sources 9–10] D+T pooled RCT AEs in % [sources 5–6]
Rash 4.91 0.72
Diarrhea 9.58 0.89
Colitis 9.83 0.00
Nausea 1.97 0.18
Vomiting 2.21 0.89
Arthralgia 0.25 0.72
CuSCC 0.00 1.97
Pyrexia 1.23 5.37
Decreased ejection fraction 0.00 2.86
Increase in AST 8.11 1.07
Increase in ALT 7.13 0.72
Constipation 0.25 0.00
Fatigue 4.42 0.72
Pruritus 1.72 0.00
Decreased appetite 0.98 0.00
Hyperthyroidism 0.25 0.00
Headache 0.74 0.00
Hypophysitis 0.49 0.00
Pneumonitis 0.49 0.00
Maculopapular rash 0.74 0.00
Dyspnea 1.23 0.00
Odema peripheral 0.00 0.36
Bleeding events 0.00 0.18
Non-cutaneous malignancies 0.00 0.18
New primary melanoma 0.00 0.18
Hand–foot syndrome 0.00 0.18
Chills 0.00 0.54
Increased lipase 1.97 0.00